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Rhythmically Entrained Exercise in Community-Dwelling Older Adults

Not Applicable
Completed
Conditions
Exercise
Gait
Caregiver Burden
Respite Care
Mental Health
Balance
Memory Disorders
Healthy Aging
Cognitive Impairment
Psychosocial Intervention
Registration Number
NCT05462977
Lead Sponsor
University of North Carolina, Greensboro
Brief Summary

Researchers at the University of North Carolina at Greensboro conduct a single-arm intervention trial to investigate the efficacy of a music-based group exercise program for community-dwelling older adults. Up to forty participants will be recruited to participate in a music-based light-to-moderate intensity group exercise program for 20 weeks (30 - 40 min/day, up to 6 days/week), which is designed for older adults with or without functional limitations to exercise with chairs for the improvement of aerobic capacity, upper and lower body strength, and balance control at a gradually increasing pace. During the exercise sessions, participants will be trained to move in time with music playlists in synchronous tempos. Primary outcomes are cognitive performance, mobility, and health-related quality of life measured before and after the intervention. Secondary outcomes are adherence to the exercise program as a potential mediator of the treatment.

Detailed Description

Researchers at the University of North Carolina at Greensboro are conducting a single-arm intervention trial to investigate the efficacy of a music-based group exercise program for community-dwelling older adults. Up to forty participants will be recruited to participate in a music-based light-to-moderate intensity group exercise program for 20 weeks (30 - 40 min/day, up to 6 days/week), which is designed for older adults with or without functional limitations to exercise with chairs for the improvement of aerobic capacity, upper and lower body strength, and balance control at a gradually increasing pace. During the exercise sessions, participants will be trained to move in time with music playlists in synchronous tempos. Primary outcomes are cognitive performance, mobility, and health-related quality of life measured before and after the intervention. Secondary outcomes are adherence to the exercise program as a potential mediator of the treatment. The research team aims to determine whether (1) a music-based light-to-moderate intensity group exercise intervention beneficially impacts mobility, cognitive function, and health-related quality of life in community-dwelling older adults; (2) the treatment effect is mediated by adherence to physical activity; and (3) the treatment effect is moderated by cognitive impairment or functional limitations.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
18
Inclusion Criteria
  • 55 - 99 years old
  • Capable of being ambulatory with or without an assistive device.
  • No cardiac or pulmonary conditions or any neurological or musculoskeletal comorbidity or pain that would make light-intensity exercise dangerous, determined by the Physical Activity Readiness Questionnaire for Everyone or confirmed by their local medical practitioner if necessary.
  • Having adequate hearing for a conversation (including with hearing aids)
  • Capable of following the study procedures
  • No severe anxiety or depression
  • Mild to moderate cognitive impairment
Exclusion Criteria
  • Age younger than 55 or older than 99
  • Severe anxiety or depression
  • Severe cognitive impairment

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Change of walking enduranceBaseline and change from baseline at month 5

Participants' gait and walking endurance will be measured by 6-Minute Walk Test

Change of health-related quality of lifeBaseline and change from baseline at month 5

EuroQol Health Questionnaire

Change of fall risksBaseline and change from baseline at month 5

Participants' fall risks will be measured by Timed Up \& Go Test

Change of balance controlBaseline and change from baseline at month 5

Participants' balance control will be measured by 4-Stage Balance Test

Change of cognitive functionBaseline and change from baseline at month 5

Participants' cognitive function will be measured through Montreal Cognitive Assessment , Flanker Inhibitory Control and Attention test, and Pattern Comparison Processing Speed Test.

Change of lower body strengthBaseline and change from baseline at month 5

Participants' lower body strength will be measured by 30-second Chair Stand Test

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UNC Greensboro

🇺🇸

Greensboro, North Carolina, United States

UNC Greensboro
🇺🇸Greensboro, North Carolina, United States

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